Increased expression of the gene for α-interferon-inducible protein in cardiomyopathic hamster heart

Eileen M. Denovan-Wright, Gregory R. Ferrier, Harold A. Robertson, Susan E. Howlett

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

7 Citas (Scopus)

Resumen

Cardiomyopathic (CRI) hamsters have a disruption in the δ-sarcoglycan gene which leads to progressive cardiac necrosis by 30 to 40 days of age, hypertrophy by 120 days, and heart failure by 250 days. We used differential display to detect other changes in mRNA levels in 30-, 60-, and 90-day-old wild-type and CM hamsters. We identified a 400-bp cDNA with sequence similarity to the human α-interferon-inducible protein (p27). This cDNA annealed with a 570-base mRNA whose steady-state levels were increased in 30-, 60-, and 90-day-old CM compared to wild-type heart. Increased expression of this hamster homolog of p27 (p27-h) was detected in CM hamster cardiac and skeletal muscle at 60 days of age but not in liver, kidney, or brain. Thus, an inherited defect in CM hamsters leads to increased expression of p27-h in advance of the development of hypertrophy and heart failure. (C) 2000 Academic Press.

Idioma originalEnglish
Páginas (desde-hasta)103-108
Número de páginas6
PublicaciónBiochemical and Biophysical Research Communications
Volumen267
N.º1
DOI
EstadoPublished - ene. 7 2000

Nota bibliográfica

Funding Information:
This work was supported by grants from the Medical Research Council of Canada and the Heart and Stroke Foundation of Nova Scotia. We thank Lorraine Hamilton, Cindy Mapplebeck, and Peter Nicholl for technical assistance. E.D-W. holds an Eli Lilly Fellowship.

ASJC Scopus Subject Areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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